Iron(II)-8-quinolinol/MCM-41-catalyzed phenol hydroxylation and reaction mechanism

Iron(II)-8-quinolino/MCM-41 is prepared. Its catalysis is studied in phenol hydroxylation using H2O2 (30%) as oxidant. The experiment shows that Iron(II)-8-quinolinol/MCM-41 has good catalytic activity and desired stability. Based on cyclic voltammetry, ESR, and UV-visible spectra studies of iron(II)-8-quinolinol complex in liquid phase, a radical substitution mechanism is proposed and used to demonstrate the experimental facts clearly. (C) 1997 Academic Press.

Structural determinants of steroids for cytochrome P450 3A4-mediated metabolism

Cytochrome P450 3A4 (CYP3A4), a major member of cytochrome P450 isoenzymes, metabolizes the majority of steroids in 6beta-position. For the purpose of determining requisite structural features of a series of structurally related steroids for CYP3A4-mediated metabolism, three-dimensional pharmacophore modeling as well as electrotopological state map were conducted for 15 steroids. Though prior studies speculated that the chemical reactivity of the allylic 6beta-position might have a greater influence on CYP3A4 selective 6-hydroxylation than steric constraints in the enzyme, our results reveal that for CYP3A4 steroidal substrates, it is not the chemical reactivity of atoms at 6beta-site, but the pharmacophoric features, i.e. the two hydrophobic rings together with two H-bond donors, that act as the key factors responsible for detemining the CYP3A4 selective 6-hydroxylation of steroids. (C) 2004 Elsevier B.V. All rights reserved.

Identification of o-phenylenediamine polymerization product catalyzed by cytochrome c

The hydrogen peroxide (H2O2) and cytochrome c-dependent oxidation of o-phenylenediamine (o-PD) was investigated by spectrophotometry and electrochemistry. The results indicated that o-PD underwent facile catalytic oxidation in the presence of cytochrome c, and that the degradation of cytochrome c by hydrogen peroxide can also be partly prevented in the presence of o-PD. The hydroxyl radical scavengers (mannitol and sodium benzoate) and oxo-heme species scavenger (uric acid) do not inhibit the oxidation, which implies that the hydroxylation of o-PD may not be involved in its oxidation. Combining with the results of the mass spectrum, elemental analysis, nuclear magnetic resonance and Fourier transform infrared spectrum of the isolated product, a conceivable structure of the product was suggested. (C) 1998 Elsevier Science B.V.

Phenol hydroxylation by iron(II) phenanthroline: The reaction mechanism

Phenol hydroxylation catalyzed by iron(II)-1,10-phenanthroline is investigated through kinetics, ESR, W-Vis as well as cyclic voltammogram studies. The optimum reaction conditions are obtained for diphenols production. Radical substitution mechanism is first proposed to explain the effects of pH, reaction medium and other factors on the phenol hydroxylation with H2O2 as oxidant, and found that the coexisting of iron(II)-1,10-phenanthroline and iron(III)-1,10-phenanthroline is the key for phenol hydroxylation to occur with H2O2 as oxygen donor.

Investigation of Catalysis of Y-Ba-Cu-O Mixed Oxides in Phenol Hydroxylation

Superconductor Y-Ba-Cu-O mixed oxides were synthesized and their catalysis in phenol hydroxylation was studied too. Results show that, Y2BaCuO5 has better activity than that of YBa2Cu3O7-x, With the catalysis study of another mixed oxide La2CuO4 a conclusion that AO structure unit is the key for mixed oxides to have high activity in phyenol hydroxylation was drawn. Meanwhile, the effects of reaction temperature, medium and medium (water) pH on phenol hydroxylation catalyzed by Y2BaCuO5 and the stability of the mixed oxides were also studied.

Genome-wide identification and characterization of cytochrome P450 monooxygenase genes in the ciliate Tetrahymena thermophila

Background: Cytochrome P450 monooxygenases play key roles in the metabolism of a wide variety of substrates and they are closely associated with endocellular physiological processes or detoxification metabolism under environmental exposure. To date, however, none has been systematically characterized in the phylum Ciliophora. T. thermophila possess many advantages as a eukaryotic model organism and it exhibits rapid and sensitive responses to xenobiotics, making it an ideal model system to study the evolutionary and functional diversity of the P450 monooxygenase gene family. Results: A total of 44 putative functional cytochrome P450 genes were identified and could be classified into 13 families and 21 sub-families according to standard nomenclature. The characteristics of both the conserved intron-exon organization and scaffold localization of tandem repeats within each P450 family clade suggested that the enlargement of T. thermophila P450 families probably resulted from recent separate small duplication events. Gene expression patterns of all T. thermophila P450s during three important cell physiological stages (vegetative growth, starvation and conjugation) were analyzed based on EST and microarray data, and three main categories of expression patterns were postulated. Evolutionary analysis including codon usage preference, sit-especific selection and gene-expression evolution patterns were investigated and the results indicated remarkable divergences among the T. thermophila P450 genes. Conclusion: The characterization, expression and evolutionary analysis of T. thermophila P450 monooxygenase genes in the current study provides useful information for understanding the characteristics and diversities of the P450 genes in the Ciliophora, and provides the baseline for functional analyses of individual P450 isoforms in this model ciliate species.

Lipase-catalyzed synthesis of biodiesel from acid oil in fixed bed reactor

Acid oil, which is a by-product in vegetable oil refining, mainly contains free fatty acids (FFAs) and acylglycerols and is a feedstock for production of biodiesel fuel now. The transesterification of acid oil and methanol to biodiesel was catalyzed by immobilized Candida lipase in fixed bed reactors. The reactant solution was a mixture of acid oil, water, methanol and solvent (hexane) and the main product was biodiesel composed of fatty acid methyl ester (FAME) of which the main component was methyl oleate. The effects of lipase content, solvent content, water content temperature and flow velocity of the reactant on the reaction were analyzed. The experimental results indicate that a maximum FAME content of 90.18% can be obtained in the end product under optimum conditions. Most of the chemical and physical properties of the biodiesel were superior to the standards for 0(#) diesel (GB/T 19147) and biodiesel (DIN V51606 and ASTM D6751).

植物细胞色素P450对土壤PAHs污染早期诊断研究

以高等植物为试验材料，建立了细胞色素P450含量的测定方法。在此基础上通过对5种植物（小麦、玉米、白菜、萝卜、大豆）的筛选试验，最终选择小麦绿苗和玉米黄化苗作为供试材料，进行土壤菲、芘单一与复合污染条件下，细胞色素P450含量与多环芳烃污染的量-效关系生态毒理诊断研究。同时为比较不同指标对污染物生态毒性敏感性，进行了相同剂量条件下，SOD、POD、CAT活性,高等植物种子发芽与根伸长抑制率与菲、芘单一与复合污染诱导的剂量-效应关系试验研究。 细胞色素P450含量污染诱导研究结果表明，在较低的浓度下，土壤菲、芘单一暴露与小麦和玉米幼苗P450含量具有显著的污染诱导剂量-效应关系，菲、芘复合污染对小麦和玉米的P450产生协同毒性作用。两种植物P450含量对菲、芘污染指示较为敏感。 SOD、POD、CAT活性比较试验结果表明，SOD、POD、CAT活性对菲、芘污染具有响应，但响应敏感性不及植物色素P450，有些不能进行定量诊断，但可用于定性诊断。 发芽率和根伸长抑制率试验比较结果表明，在同样的供试浓度范围内，小麦发芽率和根伸长与对照相当，未出现明显诱导或抑制的响应。植物色素P450含量对菲、芘单一与复合污染的指示作用比植物种子发芽率和根伸长抑制率更为敏感。 植物细胞色素P450这一敏感指标可以作为生物标记物，与化学分析及抗氧化酶系指标结合起来进行土壤PAHs早期诊断。既有助于提高指标的准确性和敏感性，推动形成完善的土壤污染生态毒理诊断方法，还可从生理和分子水平使污染诱发障碍的机理等得到破译。